CleftPALS is a volunteer based non-profit organisation of parents and professionals involved in the treatment of the cleft condition.
CleftPALS works most actively to support parents who have young children that have been born with a cleft. CleftPALS can assist with reliable and supportive information if an Ultrasound Detection of a cleft condition has occurred.
CleftPALS is also available to provide ongoing support to older children and adults who have been affected with a cleft condition. Providing phone contact and advice throughout the years. CleftPALS has been supplying services to parents whose children are born with a cleft for over 30 years throughout Australia.
CleftPALS NSW has a committee supported by regional members and contact parents. CleftPALS does not provide professional medical advice. Specific questions about treatment needs to be asked of professionals working directly with the cleft lip and palate condition relating to each patient.
If you are interested in joining our committee, please contact firstname.lastname@example.org.
|President & Contact Parent Coordinator||Jo Myers|
|Vice President||Paula Dunn|
|Equipment Coordinator||Danielle Hurdis|
|Facebook Coordinator||Emily Couchman|
|Email Coordinator||Tania McGuire|
|General Committee||Heidi Lehmann-Bird